Beilstein J. Nanotechnol.2012,3, 759–772, doi:10.3762/bjnano.3.85
include, but are not limited to, their use in targeted drug delivery and chemical sensors in the identification of oil, removal of contaminants and enhanced oil recovery (EOR). Au, iron oxide, polymer and silica nanoparticles have been studied in targeted drug delivery [3][4][5][6][7][8]. In cancer
treatment, nanoparticles are either functionalized with biomolecules that recognize and attach to the cancer cells, [6][7] or in the case of iron-oxide nanoparticles, the nanoparticles are directed by an external magnetic field [9]. The cells are destroyed by drugs that coat the nanoparticles or by
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Figure 1:
(a) Schematic of drug-carrying nanoparticles targeting cancer cells and releasing their therapeutic...
Beilstein J. Nanotechnol.2012,3, 444–455, doi:10.3762/bjnano.3.51
to the tumor site is highly desirable in cancertreatment, because it is capable of minimizing collateral damage. Herein, we report the synthesis of a nanoplatform, which is composed of a 15 ± 1 nm diameter core/shell Fe/Fe3O4 magnetic nanoparticles (MNPs) and the topoisomerase I blocker SN38 bound
the payload of tumor-homing double-stable RAW264.7 cells; (2) Release of chemotherapeutic SN38 at the cancer site by means of the self-containing Tet-On Advanced system; (3) Provide localized magnetic hyperthermia to enhance the cancertreatment, both by killing cancer cells through magnetic heating
of hyperthermia with radiation therapy and chemotherapy can greatly improve the efficacy of cancertreatment [30][31]. Ultrasmall magnetic nanoparticles generate heat efficiently in an alternating magnetic field (AMF). Due to their superior properties, such as negligible or low toxicity
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Scheme 1:
Preparation of core/shell Fe/Fe3O4 magnetic nanoparticles (MNPs).